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FDA 510(k)

MICRODERM, MODEL/VERSION 3.5

K-Number: K040171 · 2004-06-08

ApplicantVisiomed AG
Decision Date2004-06-08
Product CodePSN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRODERM, MODEL/VERSION 3.5 is the device name listed in this FDA 510(k) record. The listed applicant is Visiomed AG. It received FDA 510(k) clearance on 2004-06-08 under 510(k) number K040171. The device is classified under product code PSN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRODERM, MODEL/VERSION 3.5?

MICRODERM, MODEL/VERSION 3.5 is a medical device that received FDA 510(k) clearance on 2004-06-08. The listed applicant is Visiomed AG. The 510(k) number is K040171.

When did MICRODERM, MODEL/VERSION 3.5 receive FDA 510(k) clearance?

MICRODERM, MODEL/VERSION 3.5 received FDA 510(k) clearance on 2004-06-08, under 510(k) number K040171.

Who is the listed applicant for MICRODERM, MODEL/VERSION 3.5?

The FDA 510(k) record lists Visiomed AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRODERM, MODEL/VERSION 3.5?

The FDA product code for MICRODERM, MODEL/VERSION 3.5 is PSN.

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Related Devices (Code: PSN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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